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rs794728168

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728168(A;A)
Make rs794728168(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48513585
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728168
ebirs794728168
HLIrs794728168
Exacrs794728168
Varsomers794728168
Maprs794728168
PheGenIrs794728168
hapmaprs794728168
1000 genomesrs794728168
hgdprs794728168
ensemblrs794728168
gopubmedrs794728168
geneviewrs794728168
scholarrs794728168
googlers794728168
pharmgkbrs794728168
gwascentralrs794728168
openSNPrs794728168
23andMers794728168
23andMe allrs794728168
SNP Nexus

SNPshotrs794728168
SNPdbers794728168
MSV3drs794728168
GWAS Ctlgrs794728168
Max Magnitude0
ClinVar
Risk rs794728168(A;A)
Alt rs794728168(A;A)
Reference rs794728168(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48805782C>T
CLNSRC
CLNACC RCV000181433.2,